Suppr超能文献

对一名47,XYY男性射出精子的染色体组成进行的荧光原位杂交分析。

A fluorescent in situ hybridization analysis of the chromosome constitution of ejaculated sperm in a 47,XYY male.

作者信息

Han T H, Ford J H, Flaherty S P, Webb G C, Matthews C D

机构信息

Genetics Department, Queen Elizabeth Hospital, Woodville, South Australia.

出版信息

Clin Genet. 1994 Feb;45(2):67-70. doi: 10.1111/j.1399-0004.1994.tb03996.x.

Abstract

Two semen samples from a 47,XXY male were examined using chromosome-specific DNA probes and fluorescent in situ hybridization (FISH) to determine the distribution of sex chromosomes and an autosome (chromosome 17) in the sperm. A motile population of sperm was also prepared from one sample using the swim-up technique to compare the motile and total sperm populations. Chromosomes were localized using single FISH and a biotinylated chromosome 17 probe (TR17), or double FISH using a biotinylated X chromosome probe (TRX) and a digoxigenin-labelled Y chromosome probe (HRY). Labelling efficiencies were 95-98%. Ploidy levels were estimated by measurement against a microscope eye-piece graticule. The overall ratio of X- to Y-bearing sperm was 47% to 48.4% in the neat samples, and 48.4% to 45.3% in the swim-up fraction. Neither of the ratios was significantly different from 1:1. The frequencies of monosomic and disomic (but otherwise haploid sperm) were not different from the frequencies we observed in normal donors. In contrast, the frequencies of both diploid and tetraploid cells were increased in the neat samples of the XYY male. In the swim-up fractions, however, none of these parameters differed from those of ten normal semen donors. These results support the hypothesis that the extra Y chromosome in XYY men is eliminated during spermatogenesis.

摘要

使用染色体特异性DNA探针和荧光原位杂交(FISH)技术对一名47,XXY男性的两份精液样本进行检测,以确定精子中性染色体和一条常染色体(17号染色体)的分布情况。还使用上浮法从其中一份样本中制备了具有运动能力的精子群体,以比较有运动能力的精子群体和整个精子群体。使用单FISH和生物素化的17号染色体探针(TR17)对染色体进行定位,或使用生物素化的X染色体探针(TRX)和地高辛标记的Y染色体探针(HRY)进行双FISH。标记效率为95%-98%。通过在显微镜目镜测微尺上测量来估计倍性水平。在未处理的样本中,携带X染色体与携带Y染色体的精子总体比例为47%至48.4%,在上浮部分中为48.4%至45.3%。这两个比例均与1:1无显著差异。单体和二体(但其他方面为单倍体精子)的频率与我们在正常供体中观察到的频率没有差异。相比之下,XYY男性未处理样本中,二倍体细胞和四倍体细胞的频率均有所增加。然而,在上浮部分中,这些参数与十名正常精液供体的参数均无差异。这些结果支持了这样的假设,即XYY男性额外的Y染色体在精子发生过程中被消除。

相似文献

10
Detection of numerical chromosome abnormalities in human spermatozoa by three-color fluorescence in situ hybridization.
J Obstet Gynaecol Res. 1998 Dec;24(6):385-92. doi: 10.1111/j.1447-0756.1998.tb00113.x.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验